Canonical Allele Identifier: PA645425101
Gene: SLC17A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 357921
ClinVar RCV Id: RCV000274133 RCV001095270
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036566.1:p.Val453Gly
CA10627556
NM_012434.5:c.1358T>G